Stem cell models of Alzheimer’s disease: progress and challenges
Abstract A major challenge to our understanding of the molecular mechanisms of Alzheimer’s disease (AD) has been the lack of physiologically relevant in vitro models which capture the precise patient genome, in the cell type of interest, with physiological expression levels of the gene(s) of interes...
Main Authors: | , , |
---|---|
Format: | Article |
Language: | English |
Published: |
BMC
2017-06-01
|
Series: | Alzheimer’s Research & Therapy |
Subjects: | |
Online Access: | http://link.springer.com/article/10.1186/s13195-017-0268-4 |
id |
doaj-d1d7dc0400d54b04a411337757850849 |
---|---|
record_format |
Article |
spelling |
doaj-d1d7dc0400d54b04a4113377578508492020-11-25T00:46:08ZengBMCAlzheimer’s Research & Therapy1758-91932017-06-019111710.1186/s13195-017-0268-4Stem cell models of Alzheimer’s disease: progress and challengesCharles Arber0Christopher Lovejoy1Selina Wray2Department of Molecular Neuroscience, UCL Institute of NeurologyDepartment of Molecular Neuroscience, UCL Institute of NeurologyDepartment of Molecular Neuroscience, UCL Institute of NeurologyAbstract A major challenge to our understanding of the molecular mechanisms of Alzheimer’s disease (AD) has been the lack of physiologically relevant in vitro models which capture the precise patient genome, in the cell type of interest, with physiological expression levels of the gene(s) of interest. Induced pluripotent stem cell (iPSC) technology, together with advances in 2D and 3D neuronal differentiation, offers a unique opportunity to overcome this challenge and generate a limitless supply of human neurons for in vitro studies. iPSC-neuron models have been widely employed to model AD and we discuss in this review the progress that has been made to date using patient-derived neurons to recapitulate key aspects of AD pathology and how these models have contributed to a deeper understanding of AD molecular mechanisms, as well as addressing the key challenges posed by using this technology and what progress is being made to overcome these. Finally, we highlight future directions for the use of iPSC-neurons in AD research and highlight the potential value of this technology to neurodegenerative research in the coming years.http://link.springer.com/article/10.1186/s13195-017-0268-4Alzheimer’s diseaseInduced pluripotent stem cellsNeuronal differentiation3D cerebral organoids |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Charles Arber Christopher Lovejoy Selina Wray |
spellingShingle |
Charles Arber Christopher Lovejoy Selina Wray Stem cell models of Alzheimer’s disease: progress and challenges Alzheimer’s Research & Therapy Alzheimer’s disease Induced pluripotent stem cells Neuronal differentiation 3D cerebral organoids |
author_facet |
Charles Arber Christopher Lovejoy Selina Wray |
author_sort |
Charles Arber |
title |
Stem cell models of Alzheimer’s disease: progress and challenges |
title_short |
Stem cell models of Alzheimer’s disease: progress and challenges |
title_full |
Stem cell models of Alzheimer’s disease: progress and challenges |
title_fullStr |
Stem cell models of Alzheimer’s disease: progress and challenges |
title_full_unstemmed |
Stem cell models of Alzheimer’s disease: progress and challenges |
title_sort |
stem cell models of alzheimer’s disease: progress and challenges |
publisher |
BMC |
series |
Alzheimer’s Research & Therapy |
issn |
1758-9193 |
publishDate |
2017-06-01 |
description |
Abstract A major challenge to our understanding of the molecular mechanisms of Alzheimer’s disease (AD) has been the lack of physiologically relevant in vitro models which capture the precise patient genome, in the cell type of interest, with physiological expression levels of the gene(s) of interest. Induced pluripotent stem cell (iPSC) technology, together with advances in 2D and 3D neuronal differentiation, offers a unique opportunity to overcome this challenge and generate a limitless supply of human neurons for in vitro studies. iPSC-neuron models have been widely employed to model AD and we discuss in this review the progress that has been made to date using patient-derived neurons to recapitulate key aspects of AD pathology and how these models have contributed to a deeper understanding of AD molecular mechanisms, as well as addressing the key challenges posed by using this technology and what progress is being made to overcome these. Finally, we highlight future directions for the use of iPSC-neurons in AD research and highlight the potential value of this technology to neurodegenerative research in the coming years. |
topic |
Alzheimer’s disease Induced pluripotent stem cells Neuronal differentiation 3D cerebral organoids |
url |
http://link.springer.com/article/10.1186/s13195-017-0268-4 |
work_keys_str_mv |
AT charlesarber stemcellmodelsofalzheimersdiseaseprogressandchallenges AT christopherlovejoy stemcellmodelsofalzheimersdiseaseprogressandchallenges AT selinawray stemcellmodelsofalzheimersdiseaseprogressandchallenges |
_version_ |
1725266755007283200 |